Antibiotic use and the risk of flare of inflammatory bowel disease

被引:33
作者
Aberra, FN
Brensinger, CM
Bilker, WB
Lichtenstein, GR
Lewis, JD
机构
[1] Univ Penn, Sch Med, Div Gastroenterol, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Ctr Clin Epidemiol & Biostat, Philadelphia, PA 19104 USA
[3] Vet Affairs Med Ctr, Philadelphia, PA USA
关键词
D O I
10.1016/S1542-3565(05)00020-0
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Intestinal microbial flora participate in the pathogenesis of inflammatory bowel disease. Because antibiotic therapy alters intestinal microbial flora, we hypothesized that use of antibiotics might decrease the risk of flare. Methods: We conducted a case-crossover study by using the General Practice Research Database from 1989-1997. Flares of disease were identified by receipt of a new prescription for either corticosteroids or mesalamine medications after an interval of at least 4 months without prescriptions for either class of medication. The primary exposure was receipt of any antibiotics in the 60 days preceding the index date. Results: Among 1205 patients with Crohn's disease, exposure to antibiotics was associated with a reduced risk of flare (adjusted odds ratio [OR], 0.78; 95% confidence interval [CI], 0.64-0.96; P =.019). The effect was strongest with more recent exposure (test for trend, P <.05). Among 2230 patients with ulcerative colitis, use of any antibiotics within 60 days was not associated with flare of disease (adjusted OR, 0.96; 95% Cl, 0.82-1.12; P =.581), although a potentially protective effect was observed in those patients with very recent exposure (exposure within 15 days: OR, 0.66; 95% Cl, 0.51-0.85). Conclusions: Antibiotic use within 60 days was associated with a lower risk of flare of Crohn's disease, but not ulcerative colitis. The strength of the protective effect of antibiotics in Crohn's disease wanes over time.
引用
收藏
页码:459 / 465
页数:7
相关论文
共 36 条
[11]   SUPPRESSION OF CELL-MEDIATED-IMMUNITY BY METRONIDAZOLE [J].
GROVE, DI ;
MAHMOUD, AAF ;
WARREN, KS .
INTERNATIONAL ARCHIVES OF ALLERGY AND APPLIED IMMUNOLOGY, 1977, 54 (05) :422-427
[12]   CARD15/NOD2 functions as an antibacterial factor in human intestinal epithelial cells [J].
Hisamatsu, T ;
Suzuki, M ;
Reinecker, HC ;
Nadeau, WJ ;
McCormick, BA ;
Podolsky, DK .
GASTROENTEROLOGY, 2003, 124 (04) :993-1000
[13]   Lessons to be learned from the NOD2 gene in Crohn's disease [J].
Hugot, JP ;
Zouali, H ;
Lesage, S .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 2003, 15 (06) :593-597
[14]   VALIDATION OF INFORMATION RECORDED ON GENERAL-PRACTITIONER BASED COMPUTERIZED DATA RESOURCE IN THE UNITED-KINGDOM [J].
JICK, H ;
JICK, SS ;
DERBY, LE .
BRITISH MEDICAL JOURNAL, 1991, 302 (6779) :766-768
[15]  
Leiper K, 2000, ALIMENT PHARM THER, V14, P801
[16]   Validity and completeness of the General Practice Research Database for studies of inflammatory bowel disease [J].
Lewis, JD ;
Brensinger, C ;
Bilker, WB ;
Strom, BL .
PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2002, 11 (03) :211-218
[17]   Seasonal variation in flares of inflammatory bowel disease [J].
Lewis, JD ;
Aberra, FN ;
Lichtenstein, GR ;
Bilker, WB ;
Brensinger, C ;
Strom, BL .
GASTROENTEROLOGY, 2004, 126 (03) :665-673
[18]   The bacterial flora in inflammatory bowel disease: Current insights in pathogenesis and the influence of antibiotics and probiotics [J].
Linskens, RK ;
Huijsdens, XW ;
Savelkoul, PHM ;
Vandenbroucke-Grauls, CMJE ;
Meuwissen, SGM .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2001, 36 :29-40
[19]   THE VAMP RESEARCH MULTIPURPOSE DATABASE IN THE UK [J].
LIS, Y ;
MANN, RD .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 1995, 48 (03) :431-443
[20]   MULTIPLE-DOSE PHARMACOKINETICS OF CEFPROZIL AND ITS IMPACT ON INTESTINAL FLORA OF VOLUNTEERS [J].
LODE, H ;
MULLER, C ;
BORNER, K ;
NORD, CE ;
KOEPPE, P .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (01) :144-149